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. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Arthritis Care Res (Hoboken). 2019 Jan;71(1):134–141. doi: 10.1002/acr.23584

Table 3:

Analysis of 426 Antiphospholipid Antibody (aPL)-positive Patients Without Other Systemic Autoimmune Diseases, Stratified by Hydroxychloroquine (HCQ) Use

Variables, n (%) HCQ Users (n:164) HCQ Non-users (n:262) p

Clinical Profile

Thrombotic APS 89 (54%) 148 (57%) 0.65
  • Arterial Thrombosis 52 (32%) 87 (33%) 0.84
  • Venous Thrombosis 75 (46%) 110 (42%) 0.3
  • Mictothrombosis 11 (7%) 16 (6%) 0.74
Obstetric APS 16 (10%) 28 (11%) 0.76
Thrombotic and Obstetric APS 21 (13%) 37 (14%) 0.70
3 out of 11 ACR SLE criteria 42 (26%) 17 (7%) <0.001

Laboratory Profile

Persistent Triple aPL-positive 60 (37%) 98 (37%) 0.87
Persistent Double aPL-positive 54 (33%) 67 (26%) 0.1
Persistent Single aPL-positive 50 (30%) 97 (27%) 0.16
ANA Positive* 102 (62%) 86 (33%) <0.001
Anti-dsDNA Positive* 30 (18%) 10 (4%) <0.001
Anti-Sm Positive* 5 (3%) 0 (0%) 0.008
Low Complement C3** 17/66 (26%) 12/60 (20%) 0.44
Low Complement C4** 20/66 (30%) 10/60 (17%) 0.02
*

Patients were considered positive for ANA, anti-dsDNA, or anti-Sm antibodies if they were ever tested positive for these antibodies.

**

“Low complement C3/C4” was determined based on: a) the levels below normal; and b) the most recent C3/4 tests before the registry entry.